| Literature DB >> 17098551 |
Kentaro Matsubara1, Kenji Matsumoto, Kaori Kameyama, Hideaki Obara, Masaki Kitajima.
Abstract
Takayasu arteritis (TA), a primary arteritis of unknown cause, commonly affects the aorta and its main branches. Most patients with TA have stenotic or occlusive changes; aneurysmal degeneration is relatively rare, and renal artery aneurysms are extremely rare. We observed a fusiform, 7-cm renal artery aneurysm in a 57-year-old man with TA who had been followed up for 17 years. The patient underwent nephrectomy and resection of the aneurysm. Histologic examinations of resected specimens of the lesion showed characteristics typical of TA.Entities:
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Year: 2006 PMID: 17098551 DOI: 10.1016/j.jvs.2006.07.016
Source DB: PubMed Journal: J Vasc Surg ISSN: 0741-5214 Impact factor: 4.268